Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene

Pediatric Neurology

Volumn 50, Issue 6, 2014, Pages 622-624

  Triantafyllou, Panagiota ^a   Economou, Marina ^a   Vlachaki, Euthymia ^b   Aggelaki, Maria ^c   Athanassiou Mataxa, Miranta ^a   Michelakaki, E ^d   Zafeiriou, Dimitrios I ^a  

^a ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

^b Aristotle University and Hippokration General Hospital   (Greece)

^c Agios Pavlos Hospital   (Greece)

^d Institute of Child Health   (Greece)

Author keywords

adrenoleukodystrophy; adrenomyeloneuropathy; growth hormone deficiency; thyroiditis; X linked

Indexed keywords

CLONIDINE; CORTICOTROPIN; FERRITIN; GLUCAGON; GROWTH HORMONE; HEMOGLOBIN; PROTEIN; PROTEIN ABCD1; SOMATOMEDIN C; THYROXINE; UNCLASSIFIED DRUG; ABC TRANSPORTER; ABCD1 PROTEIN, HUMAN;

ADRENAL INSUFFICIENCY; ADRENOLEUKODYSTROPHY; ADULT; ARTICLE; BLOOD TRANSFUSION; CASE REPORT; CORTICOTROPIN BLOOD LEVEL; DNA DETERMINATION; ENDOCRINE DISEASE; EVOKED SOMATOSENSORY RESPONSE; FATIGUE; FERRITIN BLOOD LEVEL; GAIT; GENE MUTATION; GROWTH HORMONE DEFICIENCY; HEMATOPOIESIS; HEMOGLOBIN BLOOD LEVEL; HEMOSIDEROSIS; HORMONE SUBSTITUTION; HUMAN; HYPOTHYROIDISM; MALAISE; MALE; NAUSEA AND VOMITING; PARESTHESIA; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROVOCATION TEST; QUADRIPLEGIA; RIGIDITY; THALASSEMIA; TIBIAL NERVE; YOUNG ADULT; DEFICIENCY; GENETICS; PATHOPHYSIOLOGY; PHENOTYPE;

ADRENOLEUKODYSTROPHY; ATP-BINDING CASSETTE TRANSPORTERS; ENDOCRINE SYSTEM DISEASES; GROWTH HORMONE; HUMANS; HYPOTHYROIDISM; MALE; PHENOTYPE; YOUNG ADULT;

EID: 84901244193     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2014.01.027     Document Type: Article

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